Skip to main content
Clinical Trials/ACTRN12611000388910
ACTRN12611000388910
Not yet recruiting
未知

To assess the effectiveness of lifestyle modification messages delivered by SMS to patients following non-fatal cardiac events in reducing the frequency of future hospitalization for cardiovascular illness, and cardiac as well as all-cause mortality, Karachi Pakistan

Macquarie University0 sites3,400 target enrollmentApril 14, 2011

Overview

Phase
未知
Intervention
Not specified
Conditions
Coronary Heart Disease
Sponsor
Macquarie University
Enrollment
3400
Status
Not yet recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 14, 2011
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients who have been hospitalized at one of the participating tertiary care cardiac specific hospitals \- (The Karachi Institute of Heart Disease, and the National Institute of the Cardiovascular Diseases in Karachi, Pakistan) with their first event (non\-Fatal MI, CABG, PCI, stable and Unstable Angina)
  • Be of sound state of mind.
  • Willing (consent) to participate in the study.
  • Stable cardiac status on hospital discharge.
  • Subject must own a personal mobile phone with a SIM/connection registered in their name.
  • Willing to retain the same SIM/connection for the period of the study, and if had to change the phone number agreed to notify the new number to the study center.
  • No life threatening significant co\-morbidity such as terminal cancer.
  • Primary care giver, nominated by the consented patient
  • Care giver willing (consent) to participate in the study
  • Primary care giver does not have coronary artery disease

Exclusion Criteria

  • Do not give consent to participate in the study
  • Not in a stable state of mind
  • Pregnant females
  • Don’t have a personal mobile phone and not willing to acquire one.
  • Life threatening illness, e.g., terminal stage of cancer etc.
  • Primary care giver have coronary artery disease

Outcomes

Primary Outcomes

Not specified

Similar Trials